JP2010537007A5 - - Google Patents
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- JP2010537007A5 JP2010537007A5 JP2010522082A JP2010522082A JP2010537007A5 JP 2010537007 A5 JP2010537007 A5 JP 2010537007A5 JP 2010522082 A JP2010522082 A JP 2010522082A JP 2010522082 A JP2010522082 A JP 2010522082A JP 2010537007 A5 JP2010537007 A5 JP 2010537007A5
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- JP
- Japan
- Prior art keywords
- composition
- composition according
- acid
- ionomer
- parts
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 239000000203 mixture Substances 0.000 claims description 36
- 229910052751 metal Inorganic materials 0.000 claims description 25
- 239000002184 metal Substances 0.000 claims description 24
- 229920000642 polymer Polymers 0.000 claims description 24
- 229920000728 polyester Polymers 0.000 claims description 22
- 239000011574 phosphorus Substances 0.000 claims description 18
- 229910052698 phosphorus Inorganic materials 0.000 claims description 18
- 229920000554 ionomer Polymers 0.000 claims description 16
- -1 phosphorus compound Chemical class 0.000 claims description 15
- OAICVXFJPJFONN-UHFFFAOYSA-N phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 9
- 239000004952 Polyamide Substances 0.000 claims description 7
- 229920002647 polyamide Polymers 0.000 claims description 7
- 239000011528 polyamide (building material) Substances 0.000 claims description 5
- QQVIHTHCMHWDBS-UHFFFAOYSA-N Isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims description 4
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 4
- 239000000178 monomer Substances 0.000 claims description 4
- 150000003871 sulfonates Chemical class 0.000 claims description 4
- IWEATXLWFWACOA-UHFFFAOYSA-N 2,6-dimethylnaphthalene-1-carboxylic acid Chemical compound OC(=O)C1=C(C)C=CC2=CC(C)=CC=C21 IWEATXLWFWACOA-UHFFFAOYSA-N 0.000 claims description 3
- XNGIFLGASWRNHJ-UHFFFAOYSA-N Phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims description 3
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 239000011780 sodium chloride Substances 0.000 claims description 3
- GXURZKWLMYOCDX-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol;dihydroxyphosphanyl dihydrogen phosphite Chemical compound OP(O)OP(O)O.OCC(CO)(CO)CO GXURZKWLMYOCDX-UHFFFAOYSA-N 0.000 claims description 2
- BDZBKCUKTQZUTL-UHFFFAOYSA-N Triethyl phosphite Chemical compound CCOP(OCC)OCC BDZBKCUKTQZUTL-UHFFFAOYSA-N 0.000 claims description 2
- CYTQBVOFDCPGCX-UHFFFAOYSA-N Trimethyl phosphite Chemical compound COP(OC)OC CYTQBVOFDCPGCX-UHFFFAOYSA-N 0.000 claims description 2
- HVLLSGMXQDNUAL-UHFFFAOYSA-N Triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims description 2
- JYOGYPBYFYEDPE-UHFFFAOYSA-N P(=O)(O)OP(=O)O.C(C)(C)(C)C1=C(C=CC(=C1)C(C)(C)C)C=1C(=C(C(=C(C1)C1=C(C=C(C=C1)C(C)(C)C)C(C)(C)C)C1=C(C=C(C=C1)C(C)(C)C)C(C)(C)C)C1=C(C=C(C=C1)C(C)(C)C)C(C)(C)C)C1=CC=CC=C1 Chemical group P(=O)(O)OP(=O)O.C(C)(C)(C)C1=C(C=CC(=C1)C(C)(C)C)C=1C(=C(C(=C(C1)C1=C(C=C(C=C1)C(C)(C)C)C(C)(C)C)C1=C(C=C(C=C1)C(C)(C)C)C(C)(C)C)C1=C(C=C(C=C1)C(C)(C)C)C(C)(C)C)C1=CC=CC=C1 JYOGYPBYFYEDPE-UHFFFAOYSA-N 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 claims 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 11
- LSNNMFCWUKXFEE-UHFFFAOYSA-L Sulphite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 8
- 239000003381 stabilizer Substances 0.000 description 5
- MTHSVFCYNBDYFN-UHFFFAOYSA-N Diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 4
- 229910052744 lithium Inorganic materials 0.000 description 4
- 150000002009 diols Chemical class 0.000 description 3
- WHXSMMKQMYFTQS-UHFFFAOYSA-N lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 3
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-Propanediol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N 1,4-Butanediol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- YZTJKOLMWJNVFH-UHFFFAOYSA-L 2-sulfobenzene-1,3-dicarboxylate Chemical compound OS(=O)(=O)C1=C(C([O-])=O)C=CC=C1C([O-])=O YZTJKOLMWJNVFH-UHFFFAOYSA-L 0.000 description 2
- YZTJKOLMWJNVFH-UHFFFAOYSA-N 2-sulfobenzene-1,3-dicarboxylic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1S(O)(=O)=O YZTJKOLMWJNVFH-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N Adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 229920001225 Polyester resin Polymers 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 2
- 229910052787 antimony Inorganic materials 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- PDXRQENMIVHKPI-UHFFFAOYSA-N cyclohexane-1,1-diol Chemical compound OC1(O)CCCCC1 PDXRQENMIVHKPI-UHFFFAOYSA-N 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 150000003018 phosphorus compounds Chemical class 0.000 description 2
- 239000004645 polyester resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 0 *c1cc(C(O)=O)cc(C(O)=O)c1 Chemical compound *c1cc(C(O)=O)cc(C(O)=O)c1 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N 1,2-ethanediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N 1,5-Pentanediol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N 1,6-Hexanediol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- YWJNJZBDYHRABW-UHFFFAOYSA-N 2,4-dihydroxybenzene-1,3-dicarboxylic acid Chemical compound OC(=O)C1=CC=C(O)C(C(O)=O)=C1O YWJNJZBDYHRABW-UHFFFAOYSA-N 0.000 description 1
- SLXKOJJOQWFEFD-UHFFFAOYSA-N Aminocaproic acid Chemical compound NCCCCCC(O)=O SLXKOJJOQWFEFD-UHFFFAOYSA-N 0.000 description 1
- 210000000474 Heel Anatomy 0.000 description 1
- NAQMVNRVTILPCV-UHFFFAOYSA-N Hexamethylenediamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 1
- BBQFRSVTZXRYFA-UHFFFAOYSA-N P(O)OPO.C1(=CC=CC=C1)C1=CC=CC=C1 Chemical compound P(O)OPO.C1(=CC=CC=C1)C1=CC=CC=C1 BBQFRSVTZXRYFA-UHFFFAOYSA-N 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N Phosphite Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- ORLQHILJRHBSAY-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1(CO)CCCCC1 ORLQHILJRHBSAY-UHFFFAOYSA-N 0.000 description 1
- RGEJZEFEDQCADN-UHFFFAOYSA-N [2-ethyl-2-(hydroxymethyl)hexyl] dihydrogen phosphite;2,4,6-tritert-butylphenol Chemical compound CCCCC(CC)(CO)COP(O)O.CC(C)(C)C1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 RGEJZEFEDQCADN-UHFFFAOYSA-N 0.000 description 1
- FDLQZKYLHJJBHD-UHFFFAOYSA-N [3-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC(CN)=C1 FDLQZKYLHJJBHD-UHFFFAOYSA-N 0.000 description 1
- OXIKYYJDTWKERT-UHFFFAOYSA-N [4-(aminomethyl)cyclohexyl]methanamine Chemical compound NCC1CCC(CN)CC1 OXIKYYJDTWKERT-UHFFFAOYSA-N 0.000 description 1
- ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K [O-]P([O-])([O-])=O Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000007824 aliphatic compounds Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229960002684 aminocaproic acid Drugs 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 150000001923 cyclic compounds Chemical class 0.000 description 1
- PXGZQGDTEZPERC-UHFFFAOYSA-N cyclohexane-1,4-dicarboxylic acid Chemical compound OC(=O)C1CCC(C(O)=O)CC1 PXGZQGDTEZPERC-UHFFFAOYSA-N 0.000 description 1
- YESSCOKKOLMTNS-UHFFFAOYSA-L dilithium;2-sulfobenzene-1,3-dicarboxylate Chemical compound [Li+].[Li+].OS(=O)(=O)C1=C(C([O-])=O)C=CC=C1C([O-])=O YESSCOKKOLMTNS-UHFFFAOYSA-L 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- QQVIHTHCMHWDBS-UHFFFAOYSA-L isophthalate(2-) Chemical class [O-]C(=O)C1=CC=CC(C([O-])=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-L 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 description 1
- ALVZNPYWJMLXKV-UHFFFAOYSA-N nonane-1,9-diol Chemical compound OCCCCCCCCCO ALVZNPYWJMLXKV-UHFFFAOYSA-N 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920001467 poly(styrenesulfonates) Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000006479 redox reaction Methods 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 241000894007 species Species 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US95770507P | 2007-08-23 | 2007-08-23 | |
| US60/957,705 | 2007-08-23 | ||
| US9074408P | 2008-08-21 | 2008-08-21 | |
| US9086408P | 2008-08-21 | 2008-08-21 | |
| US61/090,864 | 2008-08-21 | ||
| US61/090,744 | 2008-08-21 | ||
| PCT/US2008/074092 WO2009026555A1 (en) | 2007-08-23 | 2008-08-22 | Phosphite stabilizers for ionomeric polyester compounds |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2010537007A JP2010537007A (ja) | 2010-12-02 |
| JP2010537007A5 true JP2010537007A5 (ru) | 2011-10-06 |
| JP5264909B2 JP5264909B2 (ja) | 2013-08-14 |
Family
ID=39986444
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010522082A Expired - Fee Related JP5264909B2 (ja) | 2007-08-23 | 2008-08-22 | イオノマーポリエステル化合物のためのホスファイト安定剤 |
Country Status (12)
| Country | Link |
|---|---|
| US (3) | US20090054567A1 (ru) |
| EP (1) | EP2181152B1 (ru) |
| JP (1) | JP5264909B2 (ru) |
| KR (1) | KR101524118B1 (ru) |
| CN (1) | CN101784598A (ru) |
| AU (1) | AU2008288788B2 (ru) |
| BR (1) | BRPI0815299B1 (ru) |
| CA (1) | CA2695466C (ru) |
| MX (1) | MX2010002103A (ru) |
| RU (1) | RU2480493C2 (ru) |
| WO (1) | WO2009026555A1 (ru) |
| ZA (1) | ZA201000481B (ru) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5264909B2 (ja) * | 2007-08-23 | 2013-08-14 | エンメ エ ジ・ポリメリ・イタリア・ソチエタ・ペル・アツィオーニ | イオノマーポリエステル化合物のためのホスファイト安定剤 |
| WO2010103023A1 (en) * | 2009-03-13 | 2010-09-16 | Basf Se | Stabilized blends of polyester and polyamide |
| KR20120014888A (ko) * | 2009-03-13 | 2012-02-20 | 바스프 에스이 | 폴리에스테르 및 폴리아미드의 안정화된 블렌드 |
| JP5689131B2 (ja) | 2009-10-20 | 2015-03-25 | フューチャーフューエル ケミカル カンパニーＦｕｔｕｒｅｆｕｅｌ Ｃｈｅｍｉｃａｌ Ｃｏｍｐａｎｙ | ５−スルホイソフタル酸から、低硫酸塩の５−スルホイソフタル酸・モノ−リチウム塩を調製するための、酢酸／水混合溶媒の使用 |
| MX2013009977A (es) | 2011-03-02 | 2013-10-17 | Futurefuel Chemical Co | Sales de metal de un ester dialquilico de acido 5-sulfoisoftalico y metodo para prepararlas. |
| JP2015500791A (ja) * | 2011-08-16 | 2015-01-08 | フューチャーフューエル ケミカル カンパニーＦｕｔｕｒｅｆｕｅｌ Ｃｈｅｍｉｃａｌ Ｃｏｍｐａｎｙ | ５−スルホイソフタル酸塩類とその製造方法 |
| US8809565B2 (en) | 2011-08-29 | 2014-08-19 | Futurefuel Chemical Company | 5-sulfoisophthalic acid salts and process for the preparation thereof |
| GB2549428B (en) | 2015-01-06 | 2021-12-08 | Lawter Inc | Polyamide resins for coating of sand or ceramic proppants used in hydraulic fracturing |
Family Cites Families (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS50105755A (ru) * | 1974-01-28 | 1975-08-20 | ||
| US4680371A (en) * | 1986-02-25 | 1987-07-14 | Celanese Corporation | Preparation of aromatic polyester with improved stability by addition of phosphite during preparation |
| AU628651B2 (en) * | 1989-10-13 | 1992-09-17 | Idemitsu Kosan Co. Ltd | Styrene polymer composition |
| US5138024A (en) * | 1991-01-25 | 1992-08-11 | Eastman Kodak Company | Modified polyester useful as photographic roll film support |
| US5296550A (en) * | 1991-11-01 | 1994-03-22 | Enichem S.P.A. | Impact modified polyester blends with improved polymer compatibility |
| TW297822B (ru) * | 1994-04-13 | 1997-02-11 | Ciba Geigy Ag | |
| US6066694A (en) * | 1998-03-04 | 2000-05-23 | General Electric Company | Polyester molding composition |
| US6300405B2 (en) * | 1998-06-30 | 2001-10-09 | General Electric Company | Polyester molding composition |
| US6437054B1 (en) * | 1999-02-17 | 2002-08-20 | General Electric Company | Composition of polyester sulfonate salt ionomer, polyamide and polyepoxide |
| US6001910A (en) * | 1999-04-09 | 1999-12-14 | National Starch And Chemical Investment Holding Corporation | Use of anionic or cationic plasticizers with sulfonated polyesters in hot melt formulations |
| US6500895B1 (en) * | 2000-10-13 | 2002-12-31 | General Electric Company | Thermoplastic blend comprising poly(arylene ether) and polyamide |
| JP2002294056A (ja) * | 2001-01-25 | 2002-10-09 | Mitsubishi Chemicals Corp | ポリエステル樹脂組成物及びそれからなる射出ブローボトル |
| US6908650B2 (en) * | 2001-03-02 | 2005-06-21 | Ciba Specialty Chemicals Corporation | Polyester and polyamide compositions of low residual aldehyde content |
| US6479619B1 (en) * | 2001-03-15 | 2002-11-12 | E. I. Du Pont De Nemours And Company | Sulfoisophthalic acid solution process therewith |
| US20020173591A1 (en) * | 2001-04-06 | 2002-11-21 | Chisholm Bert Ja | Polyester polyamide molding composition |
| WO2003080731A2 (en) | 2002-03-21 | 2003-10-02 | Advanced Plastics Technologies, Ltd. | Compatibilized polyester/polyamide blends |
| JP4256754B2 (ja) * | 2002-09-27 | 2009-04-22 | 富士フイルム株式会社 | ポリエステル樹脂組成物 |
| JP4677726B2 (ja) * | 2004-03-01 | 2011-04-27 | 東レ株式会社 | ポリエステル組成物及びそれからなる繊維 |
| PT2159027E (pt) * | 2004-05-18 | 2013-04-26 | M & G Polimeri Italia Spa | Grânulos de resina compartimentados e processo para tratar termicamente os referidos grânulos |
| US8465818B2 (en) * | 2005-10-07 | 2013-06-18 | M & G Usa Corporation | Polyamides and polyesters blended with a lithium salt interfacial tension reducing agent |
| KR101323835B1 (ko) * | 2005-10-25 | 2013-10-31 | 엠 앤드 지 폴리메리 이탈리아 에스.피.에이. | 폴리에스테르 및 폴리아미드의 동시 고체상 중합을 위한안정한 폴리아미드 |
| US20070135586A1 (en) * | 2005-12-09 | 2007-06-14 | Shreyas Chakravarti | Polyamide blend compositions formed article and process thereof |
| US20080076841A1 (en) * | 2006-09-11 | 2008-03-27 | Graham Packaging Company, Lp | Phosphorous containing reprocessed polymer materials, articles formed thereof, and methods of forming such articles |
| JP5264909B2 (ja) * | 2007-08-23 | 2013-08-14 | エンメ エ ジ・ポリメリ・イタリア・ソチエタ・ペル・アツィオーニ | イオノマーポリエステル化合物のためのホスファイト安定剤 |
-
2008
- 2008-08-22 JP JP2010522082A patent/JP5264909B2/ja not_active Expired - Fee Related
- 2008-08-22 BR BRPI0815299-3A patent/BRPI0815299B1/pt not_active IP Right Cessation
- 2008-08-22 CA CA2695466A patent/CA2695466C/en not_active Expired - Fee Related
- 2008-08-22 RU RU2010110807/05A patent/RU2480493C2/ru active
- 2008-08-22 CN CN200880104049A patent/CN101784598A/zh active Pending
- 2008-08-22 WO PCT/US2008/074092 patent/WO2009026555A1/en active Application Filing
- 2008-08-22 US US12/196,499 patent/US20090054567A1/en not_active Abandoned
- 2008-08-22 AU AU2008288788A patent/AU2008288788B2/en not_active Ceased
- 2008-08-22 MX MX2010002103A patent/MX2010002103A/es active IP Right Grant
- 2008-08-22 US US12/196,441 patent/US8436080B2/en active Active
- 2008-08-22 KR KR1020107006328A patent/KR101524118B1/ko active IP Right Grant
- 2008-08-22 EP EP08798545.3A patent/EP2181152B1/en not_active Not-in-force
-
2010
- 2010-01-21 ZA ZA2010/00481A patent/ZA201000481B/en unknown
- 2010-11-11 US US12/944,065 patent/US8063124B2/en not_active Expired - Fee Related
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